Beschreibung
Product Development Quality Engineer - Medical Devices - Solothurn, Switzerland
Skills:
Three or more years experience with prior experience in the design and development of medical devices or pharmaceuticals preferred.
Strong background in Product Risk Management with experience in creation, review, and approval of risk management documentation (DFMEAs and PFMEAs).
Strong analytical skills.
Required Degree/Certificates:
BS in Engineering (or science) required.
Competencies:
Proficient in Microsoft Office (Excel, Word, etc.).
Ability to effectively manage multiple priorities and tasks.
Excellent communication skills.
Overall Responsibilities:
Remediation of existing Risk Management documentation (Design & Clinical Risk Management, Risk Management Report, and Risk Management Plan) to the Product Risk Management Process.